Primary Device ID | 04063591428376 |
NIH Device Record Key | 5a864034-03c7-4a34-8206-e67925c892e7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Suprasorb P Sensitive Ag |
Version Model Number | 20cm x 20cm no border |
Catalog Number | 180019 |
Company DUNS | 849081406 |
Company Name | L&R USA INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04063591428345 [Primary] |
GS1 | 04063591428352 [Package] Package: Box [10 Units] In Commercial Distribution |
GS1 | 04063591428369 [Package] Contains: 04063591428352 Package: Case [20 Units] In Commercial Distribution |
GS1 | 04063591428376 [Package] Contains: 04063591428345 Package: Pouch [1 Units] In Commercial Distribution |
FRO | Dressing, Wound, Drug |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-09-23 |
Device Publish Date | 2021-09-15 |
04063591428376 | 20cm x 20cm no border |
04063591428321 | 15cm x 15cm no border |
04063591428291 | 10cm x 12.5cm no border |
04063591428246 | 10cm x 10cm no border |
04063591428208 | 5cm x 5cm no border |
04063591428154 | 12.5cm x 12.5cm with border |
04063591428116 | 20cm x 20cm with border |
04063591428079 | 15cm x 15cm with border |
04063591428031 | 10cm x 10cm with border |
04063591426150 | 7.5cm x 7.5cm with border |